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GNS anticorps (C-Term)

Cet anticorps anti-GNS est un anticorps Lapin Polyclonal détectant GNS dans WB. Adapté pour Humain, Souris et Rat.
N° du produit ABIN635775

Aperçu rapide pour GNS anticorps (C-Term) (ABIN635775)

Antigène

Voir toutes GNS Anticorps
GNS (Glucosamine (N-Acetyl)-6-Sulfatase (GNS))

Reactivité

  • 32
  • 7
  • 5
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Humain, Souris, Rat

Hôte

  • 29
  • 3
  • 1
Lapin

Clonalité

  • 32
  • 1
Polyclonal

Conjugué

  • 19
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GNS est non-conjugé

Application

  • 16
  • 13
  • 13
  • 11
  • 6
  • 5
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    C-Term

    Specificité

    GNS antibody was raised against the C terminal of GNS

    Purification

    Affinity purified

    Immunogène

    GNS antibody was raised using the C terminal of GNS corresponding to a region with amino acids PILRGASNLTWRSDVLVEYQGEGRNVTDPTCPSLSPGVSQCFPDCVCEDA
  • Indications d'application

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Commentaires

    GNS Blocking Peptide, (ABIN5613817), is also available for use as a blocking control in assays to test for specificity of this GNS antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of GNS antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Antigène

    GNS (Glucosamine (N-Acetyl)-6-Sulfatase (GNS))

    Autre désignation

    GNS

    Sujet

    GNS is a lysosomal enzyme found in all cells. It is involved in the catabolism of heparin, heparin sulphate, and keratan sulphate. Deficiency of this enzyme results in the accumulation of undegraded substrate and the lysosomal storage disorder ucopolysaccharidosis type IIID (Sanfilippo D syndrome). Mucopolysaccharidosis type IIID is the least common of the four subtypes of Sanfilippo syndrome.

    Poids moléculaire

    58 kDa (MW of target protein)

    Pathways

    Glycosaminoglycan Metabolic Process
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